A 14-DAY LIMIT FOR BIOETHICS: THE DEBATE OVER HUMAN EMBRYO RESEARCH


Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives

Metachromatic leukodystrophy (MLD) is a glycosphingolipid storage disease caused by deficiency of the lysosomal enzyme arylsulfatase A (ASA) or its activator protein saposin B.MLD can affect all age groups in severity varying from a severe fatal form to milder adult onset forms.Diagnosis is usually made by measuring leukocyte ASA activity.However,

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